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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529196Generated: October 30, 2026

Hydrochloric Acid → 6-Ethoxy-1,3-dihydro-1-hydroxy-2,1-benzoxaborole

https://huagongshe.com/reaction/529196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl BromideHCID 6332—
ReactantSodium hydrideHCID 24758—
Reactant1,3-Dihydro-2,1-benzoxaborole-1,6-diolHCID 52919291—
SolventDimethylformamideHCID 6228—
Product6-Ethoxy-1,3-dihydro-1-hydroxy-2,1-benzoxaboroleHCID 5135126665.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

H181 (110 mg, 0.73 mmol) was dissolved in DMF (6.0 mL) and cooled to 0° C. with ice bath. To this solution under nitrogen were added in sequence NaH (60% in mineral oil, 117 mg, 2.93 mmol) and bromoethane (0.22 mL, 2.93 mmol). The reaction mixture was stirred for 1 d then treated with 1.0 M HCl (10.0 mL). After extraction with ethyl acetate, the organic phase was washed with water and brine, and dried over anhydrous Na2SO4. The residue after rotary evaporation was purified by column chromatography over silica gel to give the title compound (85 mg, 65% yield). 1H NMR (300 MHz, DMSO-d6): δ 9.13 (s, 1H), 7.29 (d, J=8.1 Hz, 1H), 7.20 (d, J=2.4 Hz, 1H), 7.03 (dd, J=8.1 & 2.4 Hz, 1H), 4.91 (s, 2H), 4.02 (q, J=7.0 Hz, 2H) and 1.33 (t, J=7.2 Hz, 3H) ppm; Mp: 80-82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346834B2
Source datasetuspto-grants-2016_05
ORD IDord-29eda886421849d6b3341170d681ae7e
Source noteuspto-grants-2016_05